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Updated: Sep 19, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Paula Tanabe1,2, Wei Pan1,2, Audrey L Blewer1,3,4
1Duke University School of Nursing, Durham, North Carolina.
This study defines new categories for emergency department (ED) use in sickle cell disease (SCD), identifying factors like age and social vulnerability linked to super-high utilization. These definitions may change how high ED use is understood.
08:23Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
Published on: November 5, 2019
05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
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